Low cost,high efficiency flexible supercapacitor electrodes made from areca nut husk nanocellulose and silver nanoparticle embedded polyaniline

Energy storage is a key aspect in the smooth functioning of the numerous gadgets that aid easy maneuvering through modern life. Supercapacitors that store energy faradaically have recently emerged as potential inventions for which mechanical flexibility is an absolute requirement for their future applications. Flexible supercapacitors based on nanocellulose extracted from easily available waste materials via low cost methods have recently garnered great attention. In the present work, we discuss the construction of flexible, binder-free supercapacitive electrodes using nanocellulose extracted from locally available areca nut husks and polyaniline embedded with silver nanoparticles. The prepared electrodes were characterized using SEM, TEM, XRD, FTIR, EDX and electrochemical characterization techniques such as CV, galvanostatic charge–discharge, chronoamperometry and EIS. A specific capacitance of 780 F g⁻¹ was obtained for the silver nanoparticle embedded polyaniline–nanocellulose (Ag–PANI–NC) substrate supported electrodes, which is ∼4.2 times greater than that of bare polyaniline–nanocellulose electrodes. We attributed this enhancement to a lowering of the activation energy barrier of correlated electron hopping among localized defect states in the composite matrix by the Ag nanoparticles. An energy density value of 15.64 W h kg⁻¹ and a power density of 244.8 W kg⁻¹ were obtained for the prepared electrodes. It was observed that the Ag–PANI–NC based electrode can retain ∼98% of its specific capacitance upon recovery from mechanical bending to extreme degrees.

Energy storage is a key aspect in the smooth functioning of the numerous gadgets that aid easy maneuvering through modern life. Utilization of waste materials for energy storage applications enables the sustainable development of energy field.     

Construction of a ternary system: a strategy for the rapid formation of porous poly(lactic acid) fibers

Combining electrospinning technology with nonsolvent induced phase separation (ESP-NIPS), 10 wt% poly(lactic acid) (PLA) spinning solutions are prepared by using chloroform as a good solvent and absolute ethanol as a nonsolvent. The “PLA/CHCl₃/C₂H₅OH” ternary system is constituted to realize the rapid preparation of porous-structured PLA fibers. The morphologies, thermal properties and crystalline structures of the obtained fibers are characterized and the rapid forming mechanism of PLA porous fibers is investigated and discussed. The interaction parameters between the substances of the “PLA/CHCl₃/C₂H₅OH” ternary system, binodal line, spinodal line and critical point are obtained by theoretical calculation and experiment, and the “PLA/CHCl₃/C₂H₅OH” ternary phase diagram model is established. The results show that, when the mass ratio of chloroform/ethanol is around 75/25, the rapid “in situ” formation of the PLA fibers can be realized with porous structures within 5–10 s. The establishment of a “nonsolvent-solvent–polymer” ternary phase diagram model has laid a theoretical foundation for the rapid formation of polymer porous fibers by ESP-NIPS. The ESP-NIPS for the porous PLA fibers preparation provides a new resolution for the rapid formation of porous polymer materials, which is vital to further expand the application of electrospun fibers in emergency situations such as isolation, protection, insulation and flame retardant usage.

Combining electrospinning technology with ESP-NIPS, using chloroform as a solvent and absolute ethanol as a nonsolvent, poly(lactic acid) porous fibres are prepared within 5–10 s. This preparation provides a new resolution for the rapid formation of porous polymer materials.     

A supramolecular approach towards strong and tough polymer nanocomposite fibers

Polymer nanocomposite fibers are important one-dimensional nanomaterials that hold promising potential in a broad range of technological applications. It is, however, challenging to organize advanced polymer nanocomposite fibers with sufficient mechanical properties and flexibility. Here, we demonstrate that strong, tough and flexible polymer nanocomposite fibers can be approached by electrospinning of a supramolecular ensemble of dissimilar and complementary components including flexible multiwalled carbon nanotubes (CNT), and stiff cellulose nanocrystals (CNC) in an aqueous poly(vinyl alcohol) (PVA) system. CNT and CNC are bridged by a water-soluble aggregation-induced-emission (AIE) molecule that forms π–π stacking with CNT via its conjugated chains, and electrostatic attraction with CNC through its positive charges leading to a soluble CNT–AIE–CNC ensemble, which further assembles with PVA through hydrogen bonds. A high level of ordering of the nanoscale building blocks combined with hydrogen bonding leads to a more efficient stress transfer path between the reinforcing unit and the polymer. The nanocomposite fiber mat is capable of selective detection of nitroaromatic explosives.

Strong, tough and flexible polymer nanocomposite fibers can be approached by electrospinning of supramolecular ensemble of CNT–AIE–CNC/PVA in an aqueous system, which could be used for sensing.     

Deposition of an ultra-thin polyaniline coating on a TiO2 surface by vapor phase polymerization for electrochemical glucose sensing and photocatalytic degradation

Here, we have synthesized an ultra-thin coating of polyaniline on a TiO₂ nanoparticle surface (PANI–TiO₂) using a simple vapor phase polymerization method. By this method, an ultra-thin layer of PANI is obtained selectively on the TiO₂ surface. This ultra-thin coating exhibits the properties of both the parent materials due to the composite surface causing an effective synergistic effect. SEM, TEM, and EDX studies and elemental mapping confirmed the formation of ultra-thin films on the TiO₂ surface. TGA, UV/Vis and XRD studies were also done for further characterization. The composite has been used as a biosensor for glucose detection by immobilization of the enzyme glucose oxidase (GOx). Cyclic voltammetry, electrochemical impedance spectroscopy and amperometry studies were performed for glucose sensing. The linear range was observed from 20 to 140 μM glucose concentration from the amperometric analysis. The LOD of the biosensor was found to be 5.33 μM. The composite has also been used for photocatalytic degradation of the cationic dye Rhodamine B (RB). The order of degradation efficiency of RB is found to be PANI < TiO₂ < PANI–TiO₂. The synergetic effect of PANI and TiO₂ is the reason for the enhanced degradation efficiency of the composite PANI–TiO₂.

Here, we have synthesized an ultra-thin coating of polyaniline on a TiO₂ nanoparticle surface (PANI–TiO₂) using a simple vapor phase polymerization method.     

Three-dimensional crimped biodegradable poly(lactic acid) fibers prepared via melt spinning and controlled structural reorganization

Biodegradable three-dimensional crimped fibers were prepared by the side-by-side composite spinning of poly(lactic acid) (PLA) and low-melting point PLA (LM-PLA). The structural variation of the PLA/LM-PLA composite fibers during dry and wet heat treatment was explored systematically. It is shown that crystallization and disorientation were two key factors for the formation of the three-dimensional crimped structure of PLA/LM-PLA side-by-side composite fibers (SSCF). The wet heat-treated fiber has better crimp performance and fluffiness, and the crimp number, crimp ratio and crimp elasticity ratio of the treated PLA/LM-PLA SSCF with good comprehensive properties are 21 per 25 mm, 31.9% and 81.6%, which are similar to those of industrialized PET/PTT three-dimensional crimped fibers. The results of this study shed light on the development of novel three-dimensional crimped fibers with biodegradability.

Biodegradable three-dimensional crimped Poly(Lactide acid)(PLA)/low-melt point poly(Lactide acid) (LM-PLA) side-by-side composite fiber was prepared by regulating the crystallization and disorientation through dry and wet heat treatment.     

Epoxy-matrix polyaniline/p-phenylenediamine-functionalised graphene oxide coatings with dual anti-corrosion and anti-fouling performance

This research work reports on the anti-corrosion and anti-fouling properties of epoxy (E) coatings reinforced with polyaniline (PANI)/p-phenylenediamine-functionalised graphene oxide (PGO) composites. The mass ratio of graphene oxide/p-phenylenediamine in any PGO was assumed to be 1 : 1, but different PANI–PGO composites containing various loadings of PGO were prepared. An ultrasonic-assisted in situ polymerization method was employed to produce PANI–PGO at low temperature (0 °C). Several analytical and microscopical techniques, i.e., Fourier-transfer infrared (FTIR) spectroscopy, X-ray diffraction (XRD), and field emission scanning electron microscopy (FESEM), were used to confirm that PANI–PGO composites were successfully synthesized. The epoxy-based coatings (E/PANI–PGO (x), x = 0.05–0.4 g) were applied by brushing them onto carbon steel substrates, which exhibited dual anti-corrosion and anti-fouling performance. Electrochemical impedance spectroscopy (EIS) results show that E/PANI–PGO (0.2) has the highest corrosion resistance (8.87 × 10⁶ Ω cm²) after 192 h of immersion in 3.5 wt% NaCl amongst all the coatings compared with neat epoxy (1.00 × 10⁴ Ω cm²) and E/PANI (6.82 × 10³ Ω cm²). Efficient antifouling performance at the macroscopic level under simulated marine conditions was observed for the epoxy-based PANI–PGO coatings with a range of PGO compositions, in particular for the 0.1 and 0.2 g PGO coatings.

Graphene oxide (GO), GO-functionalised using p-phenylenediamine (PGO) and polyaniline (PANI)-PGO composites were successfully prepared for use in epoxy-matrix coatings for anti-corrosion and anti-fouling applications.     

Ternary composites of Ni–polyaniline–graphene as counter electrodes for dye-sensitized solar cells

Dye-sensitized solar cells (DSSCs), different in principle from the conventional solar cells based on p–n junctions, are competitively cost-effective. For development of this kind of emerging solar cell, it is very significant to reduce their cost and improve their energy conversion efficiency to the maximum extent. In this article, ternary composites (Ni–PANI–G composites) consisting of nickel nanoparticles, polyaniline (PANI), and graphene (G) were prepared for the first time and used as counter electrodes to replace the noble metal Pt in DSSCs. In the case of PANI, the introduction of Ni nanoparticles can improve the electrocatalytic ability for the reduction of triiodide ions in the counter electrode, while in the meantime, the addition of graphene in the Ni–PANI–G composites can increase the electrical conductivity of the counter electrode. The optimized DSSCs fabricated by using the Ni–PANI–G composites as the counter electrode exhibit an overall power conversion efficiency of 5.80% compared to 5.30% for reference platinum (Pt) counter-electrodes. Electrochemical impedance spectra (EIS) show that the charge-transfer resistance at the interface between electrolyte and counter-electrode in the case of the ternary composite is obviously decreased. These results are significant to develop low-cost counter electrode materials for DSSCs.

In this article, ternary composites (Ni–PANI–G composites) consisting of nickel nanoparticles, polyaniline (PANI), and graphene (G) were prepared for the first time and used as counter electrodes to replace the noble metal Pt in DSSCs.     

Cotton-like micro- and nanoscale poly(lactic acid) nonwoven fibers fabricated by centrifugal melt-spinning for tissue engineering

Biodegradable materials in the form of nonwoven fibers have attracted increasing attention for tissue engineering applications because they offer large surface areas and interconnected networks. In this study, cotton-like nonwoven poly(lactic acid) (PLA) fibers were successfully fabricated by centrifugal melt-spinning. The effects of centrifugal speed and secondary melt-spinning processing on the morphology, mechanical properties, and cell compatibility of the fibers were investigated. Scanning electron microscopy, differential scanning calorimetry, and Fourier-transform infrared spectroscopy (FTIR), as well as cell culturing of MC3T3-E1 were used in this study. The results showed that centrifugal speeds from 350 to 1500 rpm satisfied the needs for fiber formation. The PLA fibers we prepared had three-dimensional structures with extensive diameter distribution from the nanoscale to several tens of micrometers, large pore sizes, and high porosities, significantly different from fibers produced by electrospinning. The fiber diameters and mechanical properties could be manipulated by controlling the centrifugal speed. The finest fibers were generated at 900 rpm with average diameters of 3.47 ± 3.48 μm. The fibers created by centrifugal melt-spinning exhibited lower cytotoxicity and higher cell proliferation than those obtained by electrospinning.

Schematic of the centrifugal melt spinning apparatus, consisting of (a) a rotary disk, (b) heating circuit, (c) electromotor, (d) filling inlet and (e) rotary collector on a drum.     

Interrogating solar photoelectrocatalysis on an exfoliated graphite–BiVO4/ZnO composite electrode towards water treatment

A novel photoanode consisting of an exfoliated graphite–BiVO₄/ZnO heterostructured nanocomposite was fabricated. The material was characterised with scanning electron microscopy (SEM), energy dispersive spectrometry (EDS) and X-ray diffraction (XRD). Photoelectrochemical studies were carried out with cyclic/linear sweep voltammetry and chronoamperometry. The solar photoelectrochemical properties of the heterojunction photoanode were investigated through the degradation of rhodamine B in water. The results revealed that the nanoparticles of BiVO₄ and ZnO were well entrapped within the interlayers of the exfoliated graphite (EG) sheets. Improved charge separation was achieved in the EG–BiVO₄/ZnO composite electrode which resulted in superior photoelectrochemical performance than individual BiVO₄ and ZnO electrodes. A higher degradation efficiency of 91% of rhodamine B was recorded using the composite electrode with the application of 10 mA cm⁻² current density and a solution pH of 7. The highest total organic carbon removal of 74% was also recorded with the EG–BiVO₄/ZnO. Data from scavenger studies were used to support the proposed mechanism of degradation. The electrode has high stability and reusability and hence lends itself to applications in photoelectrocatalysis, especially in water treatment.

Band alignment between ZnO and BiVO₄ on exfoliated graphite (EG) support.     

Characterization of three-point bending properties of metal–resin interpenetrating phase composites

Metal–resin composites provide improved combinations of mechanical properties of raw materials. A novel metal–resin interpenetrating phase composite (IPCs) has been fabricated by spontaneously infiltrating unsaturated polyester resin into porous short-fiber preforms under vacuum conditions. In this study, three-point bending experiments are performed to characterize the bending properties of the IPCs. The fractographs after bending are examined to distinguish their characteristics. The flexural strength increases almost linearly from 42 ± 4 MPa to 119 ± 5 MPa in the in-plane direction and 59 ± 4 MPa to 151 ± 8 MPa in the through-thickness direction with an increasing fiber fraction ranging from 16.78 vol% to 32.11 vol%. The structures and bending properties of the IPCs exhibit significant anisotropy. Compared with the in-plane direction, higher bending strength and flexural modulus with smaller displacement at maximum bending force are observed in the through-thickness direction. The finer fibers contribute to improving the flexural strength (from 76 ± 6 MPa to 98 ± 5 MPa for the IPCs with about 23 vol% fiber fraction from 160 μm to 90 μm fiber diameters in the in-plane directions) and modulus. The fracture of the IPC after bending presents different appearances in different directions and the anisotropy becomes less severe with decreasing fiber fraction. Resin fracture, fiber necking and fracture, and debonding are the main fracture mechanisms.

Three-point bending properties of the metal–resin IPCs exhibit anisotropy. Flexural strength increases with increasing fiber fractions and finer fibers improve the properties. The fracture shows both brittle and plastic characteristics.     

Synthesis of TiO2–ZnS nanocomposites via sacrificial template sulfidation and their ethanol gas-sensing performance

TiO₂–ZnS core–shell composite nanorods were synthesized by using ZnO as a sacrificial shell layer in a hydrothermal reaction. ZnO thin films of different thicknesses were sputter-deposited onto the surfaces of TiO₂ nanorods as templates for hydrothermally synthesizing TiO₂–ZnS core–shell nanorods. Structural analysis revealed that crystalline TiO₂–ZnS composite nanorods were formed without any residual ZnO phase after hydrothermal sulfidation in the composite nanorods. The thickness of the ZnO sacrificial shell layer affected the surface morphology and sulfur-related surface defect density in hydrothermally grown ZnS crystallites of TiO₂–ZnS composite nanorods. Due to the distinctive core–shell heterostructure and the heterojunction between the TiO₂ core and the ZnS shell, TiO₂–ZnS core–shell nanorods exhibited ethanol gas-sensing performance superior to that of pristine TiO₂ nanorods. An optimal ZnO sacrificial shell layer thickness of approximately 60 nm was found to enable the synthesis of TiO₂–ZnS composite nanorods with satisfactory gas-sensing performance through sulfidation. The results demonstrated that hydrothermally derived TiO₂–ZnS core–shell composite nanorods with a sputter-deposited ZnO sacrificial shell layer are promising for applications in gas sensors.

TiO₂–ZnS core–shell composite nanorods were synthesized by using ZnO as a sacrificial shell layer in a hydrothermal reaction.     

Enhanced photoelectrochemical biosensing performance for Au nanoparticle–polyaniline–TiO2 heterojunction composites

A new photoelectrochemical (PEC) sensing platform comprising TiO₂ nanotube arrays (TiONTAs), polyaniline (PANI), and gold nanoparticles (AuNPs) was successfully fabricated. After loading the enzyme, this Au–PANI–TiONTA electrode showed excellent response to glucose at a linear range of 2–36 mM with a 0.02 mM detection limit. Good PEC performance was obtained due to the following advantages of the material: high visible-light harvesting ability for excellent light trapping capacity of PANI and AuNPs, good separation of the photo-induced charges related to the specific Au–PANI–TiONTA heterostructure, efficient electrode surface reaction kinetics derived from the large specific surface area of TiONTAs and improved electrode catalytic activity. This work proposed a new and general PEC enzymatic format and can be extended to prepare different PEC biosensors for biomolecules such as DNA, proteins and substrates of oxidases.

A novel photoelectrode for glucose PEC biosensing composed of TiONTAs, PANI, and AuNPs was successfully obtained. The GOx@Au–PANI–TiONTA electrode exhibited a wide response range (2–36 mM) with a low detection limit (0.02 mM) and good stability.     

Highly permeable PVDF membrane with PS/ZnO nanocomposite incorporated for distillation process

In order to enhance the flux and wetting resistance of PVDF membranes for MD applications, we have developed a novel PVDF blend nanocomposite membrane using a polystyrene/ZnO (PS/ZnO) hybrid nanocomposite. The PS/ZnO nanocomposite was synthesized by free radical polymerization of styrene in the presence of vinyltrimethoxysilane (VTMS) grafted on the surface of ZnO nanoparticles. The blend nanocomposite membrane is fabricated via the phase inversion method and we examined the effects of the PS/ZnO nanocomposite on porosity, mechanical properties, hydrophobicity, LEPw, morphology, surface roughness and MD performance. It was found that the addition of the PS/ZnO hybrid nanocomposite (0.25, 0.5 and 0.75%) resulted in an increase in porosity (>70%), which is attributed to increased pore size and reduction of the spongy layer thickness. Furthermore, the addition of the nanocomposite also improved the surface roughness and contact angle. Comparison between the neat and modified membrane shows that with incorporation of the PS/ZnO nanocomposite, the desalination flux of 30 g L⁻¹ saline aqueous solution significantly increased and rejection reached 99.99%. Meanwhile, during 100 hours continuous desalination process, the membranes composed of 0.75% PS/ZnO hybrid nanocomposite exhibited high performance stability (15.79 kg m⁻² h⁻¹) compared with the neat PVDF membrane.

In order to enhance the flux and wetting resistance of PVDF membranes for MD applications, we have developed a novel PVDF blend nanocomposite membrane using a polystyrene/ZnO (PS/ZnO) hybrid nanocomposite.     

Electrochemical synthesis of hydroxyl group-functionalized PProDOT/ZnO for an ultraviolet photodetector

Ultraviolet (UV) detectors based on zinc oxide (ZnO) nanorods (NRs) are ideal materials for UV radiation detection. However, owing to the surface effect of ZnO NRs, their speed of photoresponse and photosensitivity need to be improved. In this study, a UV photodetector was fabricated via electrochemical coating of poly(3,4-propylenedioxythiophene) grafted with functional groups (–OH) on a hydrothermally grown ZnO NRs. For comparison, poly(3,4-propylenedioxythiophene)/ZnO composites were synthesized using the same method. The structure of the composite film was characterized by Fourier transform infrared spectroscopy (FT-IR), UV-visible spectroscopy (UV-vis), X-ray diffraction (XRD), Raman spectroscopy (Raman), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and energy dispersive X-ray spectroscopy (EDS). The effect of the polymer structure on the UV sensing ability of ZnO NRs was evaluated by fabricating a UV detector with a composite material. The structural results indicated that the PProDOT-type conductive polymer and ZnO composites were successfully synthesized. The UV photodetection results showed that the presence of functional groups (–OH) in polymer chains could enhance the responsivity of the material. The response time of the ZnO/PProDOT–OH composite was 15 s shorter than that of the ZnO/PProDOT composite. A rise in photocurrent induced an increase from 2.5 A W⁻¹ to 34.75 A W⁻¹ in the UV photoresponsivity of the ZnO/PProDOT–OH composite, compared with that of the pure ZnO NRs. The external quantum efficiency and detectivity significantly improved, the increases of which were attributed to the coupling of the polymer and ZnO NRs.

Ultraviolet (UV) detectors based on zinc oxide (ZnO) nanorods (NRs) are ideal materials for UV radiation detection.     

Fabrication and evaluation of melamine-formaldehyde resin crosslinked PVA composite coating membranes with enhanced oxygen barrier properties for food packaging

Since PVA membrane is of limited use for food packaging applications in moist conditions, polyvinyl alcohol/melamine-formaldehyde resin (PVA/MF) composite coating membranes with various contents of MF were fabricated by a chemical crosslinking method to reduce the sensitivity of PVA to moisture. The morphology, chemical structure, thermal and mechanical properties of the resultant PVA/MF composite coating membranes were characterized by scanning electron microscopy (SEM), FT-IR spectrometer, X-ray diffraction (XRD), thermal gravimetric analysis (TGA), differential scanning calorimeter (DSC) and universal testing machine. In addition, their hazes and OTRs were also measured as a function of MF content. Experimental results showed that –OH in the molecular chain of MF and PVA could be crosslinked at room temperature to form a dense polymeric structure, resulting in the increase in viscosity and the decline in water absorption. The incorporation of MF into PVA gave rise to the enhancement of crosslinking through the C–O–C bonding and strong interface interaction between MF and PVA that was beneficial to improving its thermal stability, mechanical properties and barrier properties. Furthermore, the PVA/MF composite coating membranes exhibited superior transparency due to their good leveling and wettability on both BOPET and PLA substrates. The moisture resistance and barrier properties of the MF/PVA composite coated BOPET and PLA membranes under high humidity conditions have been greatly improved, and the oxygen transmission rates (OTRs) under 75% RH could still remain at about 1.0 cm³ per m² per day. These characteristics of the PVA/MF composite coating membranes have made them exhibit widespread application prospects for coating membranes in the food packaging field.

Since PVA membrane is limited use for food packaging applications in moist conditions, PVA/MF composite coating membranes with various contents of MF were fabricated by a chemical crosslinking method to reduce the sensitivity of PVA to moisture.     

Enhanced electron transfer mediated detection of hydrogen peroxide using a silver nanoparticle–reduced graphene oxide–polyaniline fabricated electrochemical sensor

The current study aims at the development of an electrochemical sensor based on a silver nanoparticle–reduced graphene oxide–polyaniline (AgNPs–rGO–PANI) nanocomposite for the sensitive and selective detection of hydrogen peroxide (H₂O₂). The nanocomposite was fabricated by simple in situ synthesis of PANI at the surface of rGO sheet which was followed by stirring with AEC biosynthesized AgNPs to form a nanocomposite. The AgNPs, GO, rGO, PANI, rGO–PANI, and AgNPs–rGO–PANI nanocomposite and their interaction were studied by UV-vis, FTIR, XRD, SEM, EDX and XPS analysis. AgNPs–rGO–PANI nanocomposite was loaded (0.5 mg cm⁻²) on a glassy carbon electrode (GCE) where the active surface area was maintained at 0.2 cm² for investigation of the electrochemical properties. It was found that AgNPs–rGO–PANI–GCE had high sensitivity towards the reduction of H₂O₂ than AgNPs–rGO which occurred at −0.4 V vs. SCE due to the presence of PANI (AgNPs have direct electronic interaction with N atom of the PANI backbone) which enhanced the rate of transfer of electron during the electrochemical reduction of H₂O₂. The calibration plots of H₂O₂ electrochemical detection was established in the range of 0.01 μM to 1000 μM (R² = 0.99) with a detection limit of 50 nM, the response time of about 5 s at a signal-to-noise ratio (S/N = 3). The sensitivity was calculated as 14.7 μA mM⁻¹ cm⁻² which indicated a significant potential as a non-enzymatic H₂O₂ sensor.

The current study aims at the development of an electrochemical sensor based on a silver nanoparticle–reduced graphene oxide–polyaniline (AgNPs–rGO–PANI) nanocomposite for the sensitive and selective detection of hydrogen peroxide (H₂O₂).     

Nanocomposite membranes of polybenzimidazole and amine-functionalized carbon nanofibers for high temperature proton exchange membrane fuel cells

Carbon nanofibers functionalized with aminobenzoyl groups (CNF–aminobenzoyl) were prepared via direct Friedel–Crafts acylation in polyphosphoric acid. The functionalization of CNFs was characterized using XPS, FTIR, TGA, and Raman analyses. Hexafluoroisopropylidene-containing polybenzimidazole (6FPBI) composite membranes containing pristine CNFs or CNF–aminobenzoyl were prepared using solvent-assisted dispersion and solvent-casting methods. In this work, the influence of the incorporation of functionalized CNFs on several physicochemical properties of the 6FPBI nanocomposite membranes, including their thermal stability, mechanical strength, and acid doping level, was studied. The results showed that CNF–aminobenzoyl provided better mechanical reinforcement for the nanocomposite membrane, compared to pristine CNF. The SEM observation confirmed the good compatibility between the CNF–aminobenzoyl fillers and the 6FPBI matrix. For the 0.3 wt% CNF–aminobenzoyl/6FPBI composite membrane, the tensile stress was increased by 12% to be 78.9 MPa (as compared to the 6FPBI membrane), the acid doping level was improved to 12.0, and the proton conductivity at 160 °C was measured above 0.2 S cm⁻¹. Furthermore, the fuel cell performance of the membrane electrolyte assembly (MEA) for each nanocomposite membrane was evaluated. The maximum power density at 160 °C was found up to 461 mW cm⁻² for the MEA based on the 0.3 wt% CNF–aminobenzoyl/6FPBI composite membrane.

Carbon nanofibers functionalized with aminobenzoyl groups (CNF–aminobenzoyl) were prepared via direct Friedel–Crafts acylation in polyphosphoric acid.     

Ultrafast nonlinear optical properties and carrier dynamics of silver nanoparticle-decorated ZnO nanowires

Silver (Ag) nanoparticle-decorated zinc oxide (ZnO) nanowires (Ag–ZnO) have been successfully synthesized by chemical vapour deposition and the magnetron sputtering method. Scanning electron microscopy images indicate that Ag nanoparticles are distributed uniformly on the surface of the ZnO nanowires. The results of room temperature photoluminescence (RTPL) reveal two major emission peaks for the Ag–ZnO nanowires, and the emission peaks in the visible region are stronger than those of the unmodified ZnO nanowires. The mechanism of RTPL and low temperature photoluminescence (LTPL) emission is discussed in detail. Nonlinear optical properties and ultrafast dynamics have been investigated using the Z-scan and two color pump–probe (TCPP) techniques, respectively. The nonlinear absorption properties in the nano-, pico- and femto-second regime have been analyzed using the singlet state three-level and four-level models, respectively. The samples show self-focusing nonlinearity and good two-photon absorption (TPA)-induced ground state saturation absorption as well as excited state reverse saturable absorption behavior. For the nanosecond and picosecond pulses, the reverse saturated absorption in the excited state mainly originates from the absorption at low excited states or deep levels; however, for the femtosecond pulse, it is caused by the absorption at high excited states. The TCPP results show that the ground state or deep level light bleaching (for nano- and pico-second regime) and TPA-induced excited-state absorption (for femtosecond regime) behaviors range from 470 nm to 620 nm. The remarkable nonlinear optical properties reveal that Ag–ZnO nanowires are potential nanocomposite materials for the development of nonlinear optical devices.

Silver (Ag) nanoparticle-decorated zinc oxide (ZnO) nanowires (Ag–ZnO) have been successfully synthesized by chemical vapour deposition and the magnetron sputtering method.     

In situ formation of PLA-grafted alkoxysilanes for toughening a biodegradable PLA stereocomplex thin film

Poly(lactide) (PLA) has received tremendous attention recently from researchers and industrialists due to its ability to solve environmental problems related to plastic pollution. However, PLA''s brittleness, poor thermal stability, low elongation at break, and poor melt processing prevent its use in a broader spectrum of applications. Herein, we produced a very tough and thermally more stable PLA stereocomplex by simply mixing PLA with organoalkoxysilane. The stereocomplex PLA/silane (sc-PLA–silane) composite was prepared by simple mixing of three types of organoalkoxysilanes in sc-PLA followed by in situ formation of a silane-based rubbery core with a cross-linked PLA shell. Mechanical and thermal properties were improved by stereocomplexation of PLA with a small amount (1–5 wt%) of PLA-grafted silanes. The addition of organoalkoxysilane with different functional groups resulted in a plasticizer of rubbery silica-PLA core–shell gel through in situ condensation and grafting of long PLA chains at the interface between the stereocomplex and silane particles. The results revealed that the toughness of sc-PLA was improved dramatically with only a small addition (only 2.5%) of 3-(triethoxysilyl)propyl isocyanate (ICPTES). The morphology and mechanical and thermal properties of the toughened stereocomplex films were characterized. The results revealed that elongation at break was increased from 16% to 120%, while other mechanical properties such as tensile strength and modulus were retained. Surface analysis confirmed that this toughness was achieved by formation of a silica-PLA core–shell gel. The mechanical properties of PLA were improved without any significant reduction in modulus and tensile strength using this simple methodology.

Current work provides a synergistic approach to prepare super tough PLA without any significant loss of its excellent intrinsic mechanical properties.     

2D–2D ZnO/N doped g-C3N4 composite photocatalyst for antibiotics degradation under visible light

ZnO and g-C₃N₄ provide excellent photocatalytic properties for degradation of antibiotics in pharmaceutical wastewater. In this work, 2D–2D ZnO/N doped g-C₃N₄ (NCN) composite photocatalysts were prepared for degradation of tetracycline (TC), ciprofloxacin (CIP) and ofloxacin (OFLX). The addition of ZnO resulted in higher separation efficiency and lower recombination rate of photogenerated charge under visible light. The composite photocatalyst showed better degradation performance compared to ZnO or NCN alone. The TC degradation reached 81.3% in 15 minutes by applying the prepared 20% ZnO/NCN composite photocatalyst, showing great competitiveness among literature reported g-C₃N₄ based photocatalysts. After 30 minutes, the degradation rate of TC, CIP and OFLX reached 82.4%, 64.4% and 78.2%, respectively. The TC degradation constant of the composite photocatalyst was 2.7 times and 6.4 times higher than NCN and CN, respectively. Radical trapping experiments indicated that ·O₂⁻ was the dominant active substance. The transference of excited electrons from the conduction band (CB) of NCN to ZnO enhanced the separation of photogenerated electron–hole pairs and simultaneously suppressed their recombination. This study provides a possibility for the design of high-performance photocatalysts for antibiotics degradation in wastewater.

2D–2D ZnO/N doped g-C₃N₄ (NCN) composite photocatalysts were prepared for degradation of antibiotics with high efficiency.